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Metabolic crosstalk between the heart and liver impacts familial hypertrophic cardiomyopathy

Familial hypertrophic cardiomyopathy (HCM) is largely caused by dominant mutations in genes encoding cardiac sarcomeric proteins, and it is etiologically distinct from secondary cardiomyopathies resulting from pressure/volume overload and neurohormonal or inflammatory stimuli. Here, we demonstrate t...

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Detalhes bibliográficos
Main Authors: Magida, Jason A, Leinwand, Leslie A
Formato: Artigo
Idioma:Inglês
Publicado em: Backwell Publishing Ltd 2014
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3992075/
https://ncbi.nlm.nih.gov/pubmed/24567073
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/emmm.201302852
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